Evidence map›Paper›PMID 15077183›Full record

ArticleOncogene2004

The PAX8/PPARgamma fusion oncoprotein transforms immortalized human thyrocytes through a mechanism probably involving wild-type PPARgamma inhibition.

J Gregory Powell, Xiying Wang, Brandon L Allard, Mustafa Sahin, Xiao-Li Wang, Ian D Hay, Henry J Hiddinga, Seema S Deshpande, Todd G Kroll, Stefan K G Grebe and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. PAX Family, Master Regulator in Cancer.Diagnostics (Basel, Switzerland) · 2025
    Review
  3. Article
  4. Article
  5. Extracellular Vesicles as Signal Carriers in Malignant Thyroid Tumors?International journal of molecular sciences · 2022
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. TAS2R bitter taste receptors regulate thyroid function.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  14. Pax-8-PPAR-γ fusion protein in thyroid carcinoma.Nature reviews. Endocrinology · 2014
    Review
  15. Genetics and epigenetics of sporadic thyroid cancer.Molecular and cellular endocrinology · 2014
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

J Gregory PowellDepartment of Medicine, Division of Endocrinology, Mayo Clinic, Rochester, MN 55906, USA.
Xiying Wang
Brandon L Allard
Mustafa Sahin
Xiao-Li Wang
Ian D Hay
Henry J Hiddinga
Seema S Deshpande
Todd G Kroll
Stefan K G Grebe
Norman L Eberhardt
Bryan McIver
Mayo Clinic in Arizona · USAnkara University · TREmory University · USWinship Cancer Institute

Funding

TUMOR SUPPRESSORS AND DIFFERENTIATED THYROID CANCERR01CA080117 · NCI · MAYO CLINIC ROCHESTER · PI EBERHARDT, NORMAN L · 1999 to 2008
$2.0M
NCI NIH HHS CA80117
6 · The paper itself

Abstract

Follicular thyroid carcinoma (FTC) frequently harbors the PAX8/PPARgamma fusion gene (PPFP); however, its oncogenic role and mechanism(s) of action remain undefined. We investigated PPFP's effects on cell growth, apoptosis, cell-cell, and cell-matrix interactions in immortalized human thyroid cells (Nthy-ori 3-1) and NIH 3T3 cells. PPFP expression increased the growth of transient and stable Nthy-ori transfectants ( approximately threefold by 72 h). There was an 8.4% increase of cells in the S+G2/M phase, a 7.8% decrease in cells in the G0+G1 phase and a 66% decline in apoptosis at 72 h. Stable Nthy-ori PPFP transfectants grew in soft agar, and PPFP-transfected NIH 3T3 cells exhibited efficient focus formation, suggesting loss of anchorage-dependent growth and contact inhibition, respectively. Overexpression of PPARgamma in Nthy-ori cells did not recapitulate PPFP's growth effects. Treatment of Nthy-ori cells with an irreversible PPARgamma inhibitor mimicked the growth-promoting effects of PPFP and co-expression of PPFP and PPARgamma blocked PPARgamma transactivation activity. Our data provide functional evidence that PPFP acts as an oncoprotein, whose transforming properties depend in part on inhibition of PPARgamma. Our data suggest that PPFP contributes to malignant transformation during FTC oncogenesis by acting on several cellular pathways, at least some of which are normally regulated by PPARgamma.

Indexed as

Nuclear ProteinsApoptosisCell CycleCell Transformation, NeoplasticDNA-Binding ProteinsHumansPaired Box Transcription FactorsPAX8 Transcription FactorReceptors, Cytoplasmic and NuclearThyroid GlandTrans-ActivatorsTranscription FactorsDNA-Binding ProteinsNuclear ProteinsPaired Box Transcription FactorsPAX8 protein, humanPAX8 Transcription FactorReceptors, Cytoplasmic and NuclearTrans-ActivatorsTranscription Factors

Identifiers

PMID15077183
OpenAlexW1523746131

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.